NDC 63629-2343
Altavera 0.03 mg / 0.15 mg kit
On the label: Bryant Ranch Prepack. It's repackaged: Bryant Ranch Prepack rebottles it from Xiromed, LLC.'s NDC 70700-116.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aspen Oss B.V. | Oss, Netherlands | Makes the active ingredient | Problems found, fixed voluntarilyNov 24, 2022 · 3 inspections |
| Aspen Oss B.V. | Oss, Netherlands | Makes the active ingredient | Problems found, fixed voluntarilyNov 24, 2022 · 3 inspections |
Repackaging site
- Bryant Ranch Prepack, Burbank, CA, United States · repackages it and relabels it
Recalls
- Sep 18, 2018 · Class III · Xiromed LLC
Labeling: Not Elsewhere Classified: mislabeling of the Altavera generic name on the packaging component that may cause confusion.
Lots: Lots: LF11838A Expiry May 2020; LF12107A, LF12106A, Expiry June 2020
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Ethinyl Estradiol and Levonorgestrel: every company that makes it
- Form
- kit
- Strength
- 0.03 mg / 0.15 mg
- Approval
- ANDA ANDA079102
- On the market since
- Jan 1, 2018
- Package NDCs
63629-2343-1- Official label
- DailyMed (National Library of Medicine), updated Mar 2, 2023
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?